I am Living with a Diagnosis of Myelofibrosis
I was diagnosed with myelofibrosis on October 5, 2018, at the Cleveland Clinic. I'm still trying to figure it out as I had never heard of it before. I was having blood draws every week but have now increased to every 2 weeks. I’m tracking that as I was never a medical person and everything is new. Also joined an MF support group which has been very helpful!
This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The Blood-Cancer.com team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.
Community Poll
Have you taken our In America Survey yet?
Join the conversation